Go Shout Love Podcast

In this episode you will hear from Bella's parents, Thomas and Sarah. Bella is the sweetest little Nebraska gal with a contagious smile that speaks volumes into her young personality. She has been diagnosed with one of the severest forms of spina bifida. You'll hear how this little fighter never allows the challenges she faces to steal her happiness. You will also has some very real moments as the parents share their experience of hearing the diagnosis from the doctors when Sarah was still just 21 weeks gestation. These first-time parents were presented with some difficult options, including a very rare procedure.

Learn more about Bella, see her video, and support her through a purchase at www.goshout.love/Bella!

In this episode we talk to Melly and Matt brown, the parents of Silas, one of our amazing Boston area kiddos being featured in May. Silas has a unique blend of diagnoses but still lights up the room with his smile. One of the topics that the conversation focuses on which is something we haven’t talked about before is Neurostorming.

Melly and Matt share with a compelling honesty about their life and journey with Silas including some of the toughest moments and where they’ve found encouragement.

You can learn more about Silas, see his video, and support this family through a purchase at www.GoShout.Love/Silas. Every purchase in June will go towards a swing set with a special needs swing so Silas can play outside with his friends and cousins!

In this episode you have the privilege of meeting Shane and Amy, the parents of Chase and Nathan. They share honestly and openly about about the host of conditions Chase battles, and how they have navigated their journey so far relationally, emotionally, and spiritually.

You can learn more about Chase, see his video, and support this awesome kiddo through a purchase at www.GoShout.Love/Chase! Every purchase in May will help cover the cost of a stairlift for Chase.

In this episode you’ll meet Brian and Amanda, the parents of Emily, one of our featured kiddos for May from the Boston area.

They share the realities of taking home a baby that is doing all the typical baby things, only to find out on day nine of life that a significant part of her brain was missing. You’ll hear how a simple act of compassion by the doctor in that appointment left a lasting impression.

As she turns 12 this month, Emily has and is surpassing every label and expectation that has been placed on her, including living beyond her first birthday. She’s writing her own story day-by-day and inspiring many as she does.

You can learn more about Emily, see her video, and support this awesome kiddo through a purchase at www.GoShout.Love/Emily!

This episode is an honest conversation with Mark and Lacey, the awesome parents of Savannah, a happy, beautiful with conditions including Naa10 Mutation, Hydrocephalus, Epilepsy, and Eosinophilic Esophagitis (EOE). We know you'll appreciate this great conversation with two people who give a very real look into life with a child like Savannah.

You can learn more about Savannah, see her video, and support this awesome kiddo through a purchase at www.goshout.love/Savannah!

In this episode we are talking to Shelby and Patrick, the parents to Kennedy, who is one of the five beautiful Boston area kids we are shouting love for in May. They share about some of the physical and emotional challenges that come with Kennedy’s conditions, especially those associated with epilepsy. But you also hear about the beautiful growth that has happened has Kennedy has adapted to become an older sister.

You can learn more about Kennedy and support this awesome kiddo through a purchase at www.goshout.love/Kennedy!

One of the things that was special about Micah's nomination to Go Shout Love is not just the number of nominations that came in for him, but that they came in from his friends... other kids that don't see any labels when they see Micah, but simply see him as a friend. In this bonus episode we hear from these young shouters about what they've learned from Micah and how they are inspired by his journey.

Follow the lead of these awesome kids and join us in shouting love for Micah through a purchase at www.goshout.love/Micah!

In this episode we talk with Don and Chelsea, the parents of Micah, an incredible ten year old boy with a diagnosis of Spinal Muscular Atrophy (SMA) Type 1. Despite being on this rare medical journey with Micah for more than a decade, you'll immediately be able to tell that time has not reduced the passion and emotion in these amazing parents in their fight for Micah.

See their story and shout love for them through a purchase at www.goshout.love/Micah!

In this episode we meet Kyle and Lindsey, the parents of James who has an extremely rare mutation of the CNTNAP1 gene. They open up and share about the difficulty of how the excitement of James' birth quickly became a traumatic event and one of the hardest days of their lives with his unexpected diagnosis.

See their story and shout love for them through a purchase at www.goshout.love/James!

In this episode we talk to Alvaro (Al) and Ashley, the parents of Ryder and Harper - two of the five amazing kiddos we are shouting love for this month from Southern California.